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Probabilistic verification of ER stress-induced signaling pathways

机译:内质网应激诱导信号通路的概率验证

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Endoplasmic reticulum (ER) is a communication hub for several signaling and secretory pathways that regulate the cell cycle progression. Recent studies revealed that deregulation of ER stress-induced signaling pathways are involved in the patho-genesis of cancer and Alzheimers disease. Computational analysis and verification of these pathways will provide insights into the mechanism linking ER stress with different diseases. Based on the experimental observation and our recent bioinformatics studies, we construct a quantitative model to systematically study the ER stress-induced apoptosis and survival signaling pathways. To overcome the limitations of traditional simulation techniques, a formal verification method, called Probabilistic Model Checking, was introduced and applied to formally analyze the temporal logic properties of the stochastic model, which is written in the PRISM language. Compared with the symbolic model verification method, this PRISM verification technique can not only qualitatively verify the signaling pathway model using sequential probability ratio test (SPRT), but also provide a quantitative estimation of the temporal properties using confidence interval estimation method. The probabilistic verification studies show that, overexpressed ER transmembrane proteins will promote the expression of Cyclin D, Amyloid-β and MDM2, leading to the pathogenesis of cancer and other diseases in the long term, and inhibit the apoptosis. Our work also verified that, varying IKK's expression level will influence the number of NFκB molecules in the nucleus, which explained why IKK inhibitor could inhibit tumorigenesis. The proposed signaling pathway model and PRISM method can help our understanding of the mechanisms that link ER stress with cancer and other diseases.
机译:内质网(ER)是调节细胞周期进程的几种信号传导和分泌途径的交流枢纽。最近的研究表明,ER应激诱导的信号通路的失调与癌症和阿尔茨海默氏病的发病机理有关。这些途径的计算分析和验证将提供有关内质网应激与不同疾病之间联系的机制的见解。基于实验观察和我们最近的生物信息学研究,我们构建了一个定量模型来系统地研究内质网应激诱导的细胞凋亡和生存信号通路。为了克服传统仿真技术的局限性,引入了一种称为概率模型检查的形式验证方法,并将其应用到以PRISM语言编写的形式上,对随机模型的时间逻辑特性进行形式化分析。与符号模型验证方法相比,该PRISM验证技术不仅可以使用顺序概率比检验(SPRT)定性验证信号通路模型,而且可以使用置信区间估计方法对时间属性进行定量估计。概率验证研究表明,过表达的ER跨膜蛋白将促进Cyclin D,淀粉样蛋白β和MDM2的表达,长期导致癌症和其他疾病的发病,并抑制细胞凋亡。我们的工作还证实,改变IKK的表达水平将影响细胞核中NFκB分子的数量,这解释了为什么IK​​K抑制剂可以抑制肿瘤发生。拟议中的信号通路模型和PRISM方法可以帮助我们理解将内质网应激与癌症和其他疾病联系起来的机制。

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